Literature DB >> 4186041

Failure of transmission of the extra chromosome in subjects with 47,XYY karyotype.

J Melnyk, H Thompson, A J Rucci, F Vanasek, S Hayes.   

Abstract

Mesh：

Year:  1969        PMID： 4186041     DOI： 10.1016/s0140-6736(69)90504-2

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  9 in total

1.  Sperm chromosome complements in a 47,XYY man.

Authors:  J Benet; R H Martin
Journal:  Hum Genet       Date:  1988-04       Impact factor: 4.132

2.  Persistence of two Y chromosomes through meiotic prophase and metaphase I in an XYY man.

Authors:  R M Speed; M J Faed; P J Batstone; K Baxby; W Barnetson
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

3.  The prevalence of a YY synaptonemal complex over XY synapsis in an XYY man with exclusive XYY spermatocytes.

Authors:  A J Solari; G Rey Valzacchi
Journal:  Chromosome Res       Date:  1997-11       Impact factor: 5.239

4.  Meiosis and spermatogenesis in G-trisomic males.

Authors:  J Schröder; K Lydecken; A De la Chapelle
Journal:  Humangenetik       Date:  1971

5.  Normal meiosis in two 47,XYY men.

Authors:  A C Chandley; J Fletcher; J A Robinson
Journal:  Hum Genet       Date:  1976-08-30       Impact factor: 4.132

6.  Trisomy 8. Report of a mosaic human male with near-normal phenotype and normal IQ, ascertained through infertility.

Authors:  A C Chandley; T B Hargreave; J M Fletcher; M Soos; D Axworthy; W H Price
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

7.  Cytogenetic and histological studies of testicular biopsies from subfertile men with chromosome anomaly.

Authors:  M J Faed; M A Lamont; K Baxby
Journal:  J Med Genet       Date:  1982-02       Impact factor: 6.318

8.  Spermatogenesis in an infertile XYY man.

Authors:  M Faed; J Robertson; W G MacIntosh; J Grieve
Journal:  Hum Genet       Date:  1976-08-30       Impact factor: 4.132

9.  Studies of malformation syndromes in man XXXX: multiple congenital anomalies/mental retardation syndrome or variant familial developmental pattern; differential diagnosis and description of the McDonough syndrome (with XXY son from XY/XXY father).

Authors:  G Neuhäuser; J M Opitz
Journal:  Z Kinderheilkd       Date:  1975-11-13
  9 in total

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